Method and a blood oxygen tester for detecting the arterial or venous blood

ABSTRACT

A method and a blood oxygen tester for determining whether a blood sample is arterial or venous blood are disclosed. A blood oxygen tester for determining whether a blood sample is arterial or venous blood includes a housing and a blood sample receptacle defined by the housing. A blood oxygen sensor is in communication with the blood sample receptacle and a test result indicator is in communication with the blood oxygen sensor. The indicator is responsive to the blood oxygen sensor for indicating whether a tested blood sample is arterial blood or venous blood.

CROSS REFERENCE TO RELATED APPLICATION

This utility patent application is a continuation of U.S. patentapplication entitled “METHOD AND A BLOOD OXYGEN TESTER FOR DETECTING THEARTERIAL OR VENOUS BLOOD” by the same inventor, Ser. No. 12/408,238,filed Mar. 20, 2009, now U.S Pat. No. 8,080,424, issued on Dec. 20,2011, the disclosure of the aforementioned application is beingincorporated herein in its entirety by reference.

COPYRIGHT NOTICE

Portions of the disclosure of this patent document may contain materialthat is subject to copyright and/or mask work protection. The copyrightand/or mask work owner has no objection to the facsimile reproduction byanyone of the patent document or the patent disclosure, as it appears inthe Patent and Trademark Office patent file or records, but otherwisereserves all copyright and/or mask work rights whatsoever.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to medical devices in general and moreparticularly to a portable device and a method for determining whetherthe blood sample extracted from the patient's body is arterial orvenous.

2. Discussion of the Related Art

People who are extremely ill or injured are often admitted for medicalcare through a hospital's emergency room (ER). In administeringemergency care medicine in an ER, time is a very valuable commodity. Thepatient's well being and even life may depend on rapid administration ofproper medical care. Central Venous Catheters, also known as “Centrallines”, are most commonly used for administration of IV fluids,antibiotics, blood transfusions, nutritional supplements, or medicationsused to support and improve blood pressure, which are optimallydelivered through central lines. These catheters are also important forchecking serial blood tests and monitoring the fluid and hydrationstatus of the patient. In emergency and critical care medicine, thesecatheters are vital for resuscitation, monitoring, and optimalmanagement of critically ill patients.

Central line catheters are long and large bore catheters and aredesigned to be inserted into veins. Veins are low pressured and returnblood from organs and tissues to the heart and arteries are highpressured and carry oxygenated blood to organs and bodily tissues.Central lines are inserted into the large veins of the body, typicallyone of three large veins such as the internal jugular vein (located inthe neck), the subclavian vein (located in the chest), or the femoralvein (located in the groin). These large veins run next to majorarteries; the internal jugular runs alongside the carotid artery in theneck, the subclavian vein runs alongside the subclavian artery in thechest, and the femoral vein runs alongside the femoral artery in thegroin area.

To accomplish the insertion of a central line, the patient is properlypositioned and the insertion area is sterilized. The medicalprofessional uses either anatomic landmarks or ultrasound to identifythe location of the vein for insertion. The area is anesthetized and an‘introducer needle’ connected to a syringe is advanced until the tip ofthe needle is in the desired vein. Placement of the needle in the veinis confirmed by aspiration of blood into the syringe. A guide wire and adilator tube are then introduced to guide the catheter in place at whichtime the catheter is sutured in place. Appropriate positioning of thecatheter is confirmed by taking a chest x-ray.

Because of the proximity of the vein to the corresponding artery, amajor risk during the insertion of central lines is accidental arterialcannulation, or the advancement and placement of the catheter into alarge artery instead of the vein. Arterial cannulation has potentialcatastrophic implications including hemothorax (bleeding into the chestcavity), carotid, subclavian, or femoral artery injury, stroke, and evendeath. Thus, ER personnel are intent on distinguishing arterial versusvenous blood prior to cannulating with the dilator and inserting andsuturing the catheter. Current methods of distinguishing venous fromarterial blood are inaccurate, unreliable, or impractical.

The most common method of distinguishing venous from arterial bloodduring catheter placement is visual analysis. Arterial blood isclassically a brighter red and more pulsatile in comparison to venousblood. However, these characteristics are very subjective and thusunreliable. The color of a patient's blood sample can be incorrectlyinterpreted depending on a variety of factors such as the patient'sblood oxygenation, past medical history, operator experience, and eventhe ambient lighting in the room where the procedure is performed.Further, ill patients receiving central lines often have low bloodpressure who would not exhibit classic pulsatile arterial blood flow todistinguish arterial blood from venous blood.

Another method is the use of blood gas analysis. In this method, asample of blood is placed in a machine and after analysis the machinedisplays the amount of oxygenation. While accurate, blood gas analysisis not easily available and is time consuming. In many hospitals, thistest is only performed in a laboratory and can take five minutes or moreto obtain results. If the patient is in need of emergency care, propercare often requires more immediate action than available when the caregivers must wait on machine analysis.

Pressure waveform monitoring is also used to determine the source of ablood sample. However, this method is limited because most cardiacmonitors do not have this option available. Also, this method is timeconsuming to set up and requires additional people to complete theprocess. Since this method depends on the pressure of the blood sampleto distinguish between arterial and venous blood, low blood pressure insome sick patients can cause unreliable results.

Another method to aid in the placement of the catheter is the use ofultrasound. This method has been shown to reduce patient discomfort andthe number of arterial sticks. Because of the high pliancy of vesselwalls, veins tent and collapse when the central line is being placed.Even under ultrasound guidance, the medical professional can puncturethrough the vein resulting in arterial insertion. Therefore, ultrasoundguidance does not offer the reliability desired to readily distinguisharterial blood from venous blood.

Although there are various studies published in medical journals thatprovide a comparison of arterial and venous blood gas values before,during, and after the operation of the patient, none of that informationis utilized in developing a method or a device to place central linekits efficiently, safely and accurately within the patient's body. Thuswhat is desired is a testing device that can readily distinguish betweenarterial and venous blood in minimal time and at the patient's bedsidequickly and accurately to facilitate the placement of central line kitsin an emergency situation.

SUMMARY OF THE INVENTION

The present invention is directed to a blood oxygen tester thatsatisfies the need for quick and reliable testing of blood fordetermining whether a sample is arterial or venous blood at a patient'sbedside. The blood oxygen tester comprises a housing and a blood samplereceptacle defined by the housing. A blood oxygen sensor is incommunication with the blood sample receptacle and a test resultindicator is in communication with the blood oxygen sensor. Theindicator is responsive to the blood oxygen sensor for indicatingwhether a tested blood sample is arterial blood or venous blood.

Another aspect of the present invention is a blood oxygen tester fordetermining whether a blood sample is arterial or venous. The bloodoxygen tester comprises a housing having a volume of less than fiftycubic centimeters and defining a blood sample receptacle for receiving ablood sample. A blood oxygen sensor in the housing includes a reactionstrip responsive to an oxygen saturation level in the blood sample. Thehousing further defines a test result indicator in communication withthe blood oxygen sensor and is responsive to the blood oxygen sensor.The indicator displays a first color when the tested blood sample isvenous blood and a second color when the tested blood sample is arterialblood.

In another aspect of the present invention is a method for determiningwhether a patient's blood sample is venous or arterial blood utilizing ablood oxygen tester. The method includes steps of preparing a site onthe patient's body to withdraw a blood sample, inserting a needlethrough the site to withdraw the blood sample, aspirating the bloodsample, and depositing the blood sample in a receptacle of a bloodoxygen tester. The blood oxygen tester includes a blood oxygen sensorcomprising a reaction strip responsive to a certain characteristics ofthe blood. The method further includes viewing the results of the bloodsample to determine whether the blood withdrawn is arterial or venousblood. If the withdrawn blood is the venous blood, the medicalprofessional completes the insertion of a central line. If it isarterial blood, the medical professional withdraws the needle andrestarts the procedure. The reaction strip is designed to detect theoxygen saturation level or partial pressure oxygen (pO2) to identifywhether the blood withdrawn is arterial or venous.

In yet another of the present invention is a method of testing apatient's blood sample at the patient's bedside to determine whether theblood is venous or arterial blood. The method comprises the steps ofpreparing a site on the patient's body for insertion of an introducerneedle. An introducer needle is coupled with a syringe. The introducerneedle is inserted through the patient's anatomy and into a vein. Asample of blood is aspirated into the syringe. The syringe is removedfrom the introducer needle, and the blood sample is deposited in a bloodsample receptacle of a blood oxygen tester at the patient's bedside. Theblood sample is allowed to contact a blood oxygen sensor in the bloodoxygen tester comprising a reaction strip responsive to an oxygensaturation level in the blood sample. A test result indicator responsiveto the blood oxygen sensor is viewed and indicates a first color whenthe tested blood sample is venous blood and indicates a second colorwhen the tested blood sample is arterial blood.

These and other features, aspects, and advantages of the invention willbe further understood and appreciated by those skilled in the art byreference to the following written specification, claims and appendeddrawings.

BRIEF DESCRIPTION OF THE DRAWINGS

To the accomplishment of the above and related objectives, thisinvention may be embodied in the form illustrated in the accompanyingdrawings, attention being called to the fact, however, that the drawingsare illustrative only, and that changes may be made in the specificconstruction and method illustrated:

FIG. 1 is a view of a portion of a person's cardiovascular systemillustrating the proximal location of a person's veins and arteries;

FIG. 2 is a perspective view of a medical professional administering ablood sample to a blood oxygen tester embodying the present invention;

FIG. 3 is a plan view of the blood oxygen tester illustrating testresults from a venous blood sample;

FIG. 4 is a plan view of the blood oxygen tester illustrating testresults from an arterial blood sample; and

FIG. 5 is a flow chart illustrating a method of detecting a patient'sblood sample to determine whether the blood is venous or arterial.

Like reference numerals refer to like parts throughout the several viewsof the drawings.

DETAILED DESCRIPTION OF THE INVENTION

For purposes of description herein, the terms “upper”, “lower”, “left”,“rear”, “right”, “front”, “vertical”, “horizontal”, and derivativesthereof shall relate to the invention as oriented in FIG. 2. However,one will understand that the invention may assume various alternativeorientations and step sequences, except where expressly specified to thecontrary. Therefore, the specific devices and processes illustrated inthe attached drawings, and described in the following specification, aresimply various embodiments of the inventive concepts defined in theappended claims. Hence, specific dimensions and other physicalcharacteristics relating to the embodiments disclosed herein are not tobe considered as limiting, unless the claims expressly state otherwise.

Turning to the drawings, FIG. 1 shows a medical patient 10 requiring theinsertion of a central line catheter into a jugular vein 14 of apatient's neck 12. A blood sample 19 must be extracted for testing by anoxygen blood tester 20 to ensure that the catheter is being introducedto jugular vein 14 and not a carotid artery 16 located alongside jugularvein 14.

FIGS. 2-4 illustrate oxygen blood tester 20 which is one embodiment ofthe present invention and illustrates its various components. In thisembodiment, blood tester 20 includes a housing 22 that defines a bloodsample receptacle 24 for receiving a blood sample and a test resultindicator 28 for displaying the result of a blood test performed withblood tester 20. Housing 22 is of a sufficiently small size so thattester 20 can be included in pre-existing central line kits that arecommercially available (not shown). Such central line kits are readilystocked for use in medical facilities, the contents of which aredesigned for one-time use. Likewise, blood tester 20 in one embodimentis anticipated to also be a one-time use item. Housing 22 has a volumeof less than 100 cubic centimeters and ideally less than 50 cubiccentimeters for convenient use by a medical professional. In oneembodiment, the housing may be five to ten centimeters in length, threeto five centimeters in width, and less than one centimeter in height.Blood tester 20 also encloses a blood oxygen sensor 26 within housing22. Blood oxygen sensor 26 is in communication with blood samplereceptacle 24 and with test result indicator 28.

In one embodiment, the difference between the oxygen saturation ofvenous and arterial blood can be used to determine the proper placementof the central line. In the human cardiovascular system, blood iscirculated by the heart through the lungs where the blood is oxygenated.Oxygenated (arterial) blood is pumped by the heart through arteries tothe rest of the body where organs and tissue extract oxygen from theblood. Arterial blood being freshly oxygenated has a normal oxygensaturation above ninety-five percent and, in most patients, is near onehundred percent. Once the oxygenated blood reaches the organs andvarious tissue of the body, at least a portion of the oxygen is absorbedby the organs and tissues to create energy. Venous (de-oxygenated) bloodis then carried back to the heart by veins to again to be oxygenated bythe lungs. Venous blood has a normal oxygen saturation that typicallyhas a maximum of seventy-five percent oxygen saturation since oxygen hasbeen extracted from the blood by organs and tissue. Consequently, theoxygen saturation of venous blood is generally less than seventy-fivepercent whereas the oxygen saturation of arterial blood is almost alwaysabove ninety to ninety-five percent.

In this embodiment, blood oxygen sensor 26 is a reaction strip that isresponsive to the oxygen saturation level in a blood sample. Thereaction strip in sensing an oxygen saturation level corresponding tovenous blood will provide a first indication in test result indicator 28and in sensing an oxygen saturation level corresponding to arterialblood will provide a second indication distinct from the firstindication in test result indicator 28. The reaction strip can beimpregnated or coated with a reactive dye such that the reactive dyeassumes a first color 32 (FIG. 3) for display in test result indicator28 when exposed to venous blood in receptacle 24 and assumes a secondcolor 34 (FIG. 4) for display in test result indicator 28 when exposedto arterial blood in receptacle 24. The reactive dye can have a colorchange threshold corresponding to an oxygen saturation level of eightypercent, or in another embodiment, an oxygen saturation level of ninetypercent.

In another embodiment, the pO₂ differential between arterial and venousblood can also be used to determine the proper placement of the centralline. Arterial or venous blood can also be distinguished by its partialpressure of oxygen (pO₂). Before operation, arterial blood willtypically have a pO₂ level range of approximately 70-100 mmHg(millimeter of mercury) while venous blood will typically have a pO₂level range of approximately 30-40 mmHg. Thus, the pO₂ differentialbetween arterial and venous blood is significant and provides a reliableindication of which blood sample has been drawn from the patient.

In this embodiment, blood oxygen tester 20 can include sensor 26 that isreactive to the partial pressure of oxygen (pO2) in the blood sample.Sensor 26 can include a known micro-dissolved oxygen electrode that isreactive to a partial pressure of oxygen in the blood sample.Alternatively, sensor 26 can be an electro-chemical sensor that isreactive to the partial pressure of oxygen in the blood sample.

In use, blood oxygen tester 20 can be included with a central linecatheter kit to aid the medical professional in correct placement of thecatheter in one of the patient's major veins (i.e. jugular vein,subclavian vein, femoral vein). The patient is prepared for theprocedure by placing the patient's body in a desired orientation for theprocedure. The medical professional can then take appropriate sterilemeasures such as wearing a sterile gown, gloves, and mask andsterilizing the body site (i.e. neck 12) where the procedure is to beperformed. The medical professional then identifies the location of thedesired vein (i.e. jugular vein 14) by using anatomic landmarks or by anultrasound device. The procedure site can then be anesthetized. Anintroducer needle is coupled with a syringe 18 and the needle is thenadvanced through the patient's skin and tissue into jugular vein 14. Themedical professional aspirates the syringe 18 while advancing the needleuntil blood is aspirated into syringe 18. Syringe 18 is removed whilethe needle remains in place in the vein, and a sample 19 of the blood isplaced in receptacle 24 of blood oxygen tester 20.

Once blood sample 19 has been placed in receptacle 24, the medicalprofessional waits a prescribed period of time (typically a few seconds)to allow the reactive strip or sensor 26 to react to the oxygensaturation level of blood sample 19. After the expiration of theprescribed time, the result of the test is read from test resultindicator 28. If the blood sample is venous blood, test result indicator28 will display first color 32, and if the blood sample is arterialblood, test result indicator 28 will display second color 34. In thismanner, the medical professional will quickly know whether theintroducer needle has been placed in the desired vein or has beenintroduced in an undesired artery. If test result indicator 28 displayssecond color 32 indicating arterial blood, the introducer needle can berepositioned to the vein. A second blood sample is then obtained andtested on a new blood oxygen tester 20.

Once the medical professional verifies that the introducer needle iscorrectly placed in desired vein 14, a guide wire is advanced throughthe introducer needle and into the vein. The introducer needle is thenremoved and a dilator tube is advanced over the guide wire into the veinto open a tract for the catheter and then immediately removed. Thecatheter is then placed over the wire into the vein and the guide wireis removed. The ports are then flushed and sutured in place. Correctplacement of the catheter can then be confirmed by taking an x-ray ofthe area at the procedure site.

A method 100 for using blood oxygen tester 20 is shown in FIG. 5. Inblock 102, the medical professional prepares a site on a patient's bodyfor insertion of a central line. The preparation can include suchprocedures as shaving the patient's skin, sterilizing the skin surface,adding a sterile drape, etc. Once the site has been prepared, in block106 the medical professional inserts a needle through the patient's skininto a desired vein. Once the needle has been inserted into the vein, ablood sample is aspirated through the needle in block 110. Then, inblock 112 the sample is deposited in blood oxygen tester 20 and allowedto interact with sensor 26.

Once the blood sample has interacted with sensor 26, the medicalprofessional, in block 116, reads the results of the blood sample asdisplayed by indicator 28. In block 120, and in response to the displayof indicator 28, the medical professional determines if the blood sampleis arterial or venous blood. If the medical professional determines thatthe blood sample is arterial, the needle is removed in block 130 and themethod returns to block 106 for reinsertion of the needle in a desiredvein. Blocks 106 through 120 are then repeated until, as a result of theindication of display 28, the medical professional determines that theblood sample is venous. The method then proceeds to block 150. In block150, the medical professional completes the insertion of the centralline with the knowledge that the line is being inserted into a patient'svein and not into an artery.

The above description is considered that of representative embodimentsonly. Modifications of the invention will occur to those skilled in theart and to those who make or use the invention. Therefore, it isunderstood that the embodiments shown in the drawings and describedabove are merely for illustrative purposes and are not intended to limitthe scope of the invention, which is defined by the following claims asinterpreted according to the principles of patent law, including thedoctrine of equivalents.

1. A blood oxygen tester for determining whether a blood sample isarterial or venous, said blood oxygen tester comprising: a housing; ablood sample receptacle defined by said housing and having an area fordepositing a blood sample; a blood oxygen sensor within said area in theblood sample receptacle, said blood oxygen sensor reactive to a partialpressure of oxygen (pO2) in the blood sample; and a test resultindicator defined by said housing and in communication with said bloodoxygen sensor, said indicator responsive to said blood oxygen sensor'sreaction to the partial pressure of oxygen (pO2) in the deposited bloodsample displaying a first color when the blood sample is arterial bloodand indicating a second color when the blood sample is venous blood. 2.The blood oxygen tester according to claim 1, wherein said housing has avolume of less than one hundred cubic centimeters.
 3. The blood oxygentester according to claim 1, wherein said housing has a volume of lessthan fifty cubic centimeters.
 4. The blood oxygen tester according toclaim 1, wherein said blood oxygen sensor reacts to a partial pressureof oxygen (pO2) greater than seventy mmHg in the blood sample.
 5. Theblood oxygen tester according to claim 4, wherein said test resultindicator displaying the first color based on said blood oxygen sensor'sreaction to the partial pressure of oxygen (pO2) greater than seventymmHg.
 6. The blood oxygen tester according to claim 1, wherein saidblood oxygen sensor reacts to a partial pressure of oxygen (pO2) lessthan forty mmHg in the blood sample.
 7. The blood oxygen testeraccording to claim 6, wherein said test result indicator displaying thesecond color based on said blood oxygen sensor's reaction to the partialpressure of oxygen (pO2) less than forty mmHg in the blood sample.
 8. Amethod for determining whether a patient's blood sample is venous orarterial blood utilizing a blood oxygen tester, said method comprising:preparing a site on the patient's body to withdraw a blood sample;inserting a needle through the site to withdraw the blood sample;aspirating the blood sample; depositing the aspirated blood sample in areceptacle of a blood oxygen tester, said receptacle includes a bloodoxygen sensor reactive to a partial pressure of oxygen (pO2) in theblood; and viewing a color on a test result indicator to determinewhether the blood withdrawn is arterial or venous blood, said indicatordisplaying the color responsive to said blood oxygen sensor's reactionto the partial pressure of oxygen (pO2) in the deposited blood sample.9. The method according to claim 8, wherein said test result indicatordisplaying a first color when the blood sample is venous blood andindicating a second color when the blood sample is arterial blood. 10.The method according to claim 8, wherein said blood oxygen sensorincludes a micro dissolved oxygen electrode reactive to the partialpressure of oxygen in the blood sample.
 11. The method according toclaim 8, wherein said blood oxygen sensor is an electrochemical sensorreactive to the partial pressure of oxygen in the blood sample.
 12. Themethod according to claim 8, wherein said blood oxygen sensor comprisesa reaction strip reactive to the partial pressure of oxygen (pO2).
 13. Ablood oxygen tester comprising: a blood oxygen sensor reactive to apartial pressure of oxygen (pO2), wherein said blood oxygen sensorincludes a micro dissolved oxygen electrode reactive to the partialpressure of oxygen in a blood sample; and a test result indicator incommunication with said blood oxygen sensor, said indicator responsiveto said blood oxygen sensor's reaction to the partial pressure of oxygen(pO2) in a blood sample indicating whether the blood sample is arterialblood or venous blood.
 14. A blood oxygen tester comprising: a bloodoxygen sensor reactive to a partial pressure of oxygen (pO2), whereinsaid blood oxygen sensor is an electrochemical sensor reactive to thepartial pressure of oxygen in a blood sample; and a test resultindicator in communication with said blood oxygen sensor, said indicatorresponsive to said blood oxygen sensor's reaction to the partialpressure of oxygen (pO2) in a blood sample indicating whether the bloodsample is arterial blood or venous blood.
 15. The blood oxygen tester ofclaim 14, wherein said indicator indicating a first color if the bloodsample is arterial blood or a second color if the blood sample is venousblood.
 16. A blood oxygen tester comprising: a housing having a volumeof less than fifty cubic centimeters; a blood sample receptacle definedby said housing for depositing a blood sample; a blood oxygen sensorwithin said receptacle in said housing, said blood oxygen sensorreactive to a partial pressure of oxygen (pO2) in the deposited bloodsample; and a test result indicator defined by said housing and incommunication with said blood oxygen sensor, said indicator responsiveto said blood oxygen sensor's reaction to the partial pressure of oxygendisplaying a first color when the tested blood sample is venous bloodand indicating a second color when the tested blood sample is arterialblood.
 17. The blood oxygen tester of claim 16, wherein said bloodoxygen sensor includes a micro dissolved oxygen electrode reactive tothe partial pressure of oxygen in the blood sample.
 18. The blood oxygentester of claim 16, wherein said blood oxygen sensor is anelectrochemical sensor reactive to the partial pressure of oxygen in theblood sample.